concentration of solutions (molality, molarity)
TRANSCRIPT
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Chapter 10: Solutions
10. Refer to Section 10.1 and Examples 10.4 and 10.5.
Molality
Mass Percent
of Solvent Ppm Solute
Mole Fraction
of Solvent
a. 2.577 86.58% 1.340 x105 0.9556
b. 20.4 45.0 5.50 x105 0.731
c. 0.07977 99.5232% 4768 0.9986
d. 12.6 57.0% 4.30 x105 0.815
Since these are aqueous solutions, the solvent is water. The solute is urea, CO(NH2)2.
Molar mass of urea: (12.01) + 16.00 + 2(14.01 + 2(1.008)) = 60.06 g/mol.
a. 2.577 mindicates that there are 2.577 mol. of solute per 1000 g of solvent and the
calculations are based on that ratio.
ureag154.8=ureamol.1
ureag60.06mol.2.577 x
OHmol.55.49=OHg18.02
OHmol.1
kg1
g1000kg1 2
2
2xx
86.58%=g1155
g1000=100%g)154.8+g(1000
g1000=%mass x
5101.340 x=10g)154.8+g(1000
g154.8=soluteppm 6x
0.9556=mol.)2.577+mol.5.495(
mol.5.495=OH2X
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b. 45.0 mass % of solvent means that 45.0 g of solvent are present for each 100.0 g of
solution. Calculations are then based on this ratio.
OHmol.2.50=g18.02
OHmol.1g45.0 2
2x
mass of solute = 100.0 g (total) 45.0 g (water) = 55.0 g CO(NH2)2
ureamol.0.916=ureag60.06
ureamol.1ureag55.0 x
m20.4=OHkg0.0450
ureamol.0.916=molality
2
(remember to convert mass of solvent to kg)
5105.50 x=10
g100
ureag55.0=soluteppm 6x
0.731=mol.)0.916+mol..502(
mol..502=X OH2
c. g7684=10solutionofmass
soluteofmass=ppm 6x
If we assume a total mass of 106g, then the mass of solute = 4768 g by definition. Any
assumption for mass is valid here, this one was chosen for simplicity.
ureamol.9.397=ureag60.06
ureamol.1ureag4768 x
OHmol.5244.05=g18.0152
mol.1OHg952329g;952329=g4768-g10 22
6x
0.9986=mol.)79.39+mol.5244.05(
mol.5244.05=X OH2
99.5232%=100%g10
g109.95232=%mass
6
5
xx
m=kg995.232
mol.79.39=molality 0.07977
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d. Xsolvent= 0.815 indicates that there are 0.815 moles H2O per 1 mole of solvent and solute
combined. Consequently, there must be 0.185 mol. (1-0.815) urea.
ureag11.1=ureamol.1
ureag60.06ureamol.0.185 x
OHg14.7=mol.1
g18.02OHmol.0.815 22 x
m12.6=OHkg0.0147
ureamol.0.185
2
(remember to convert mass of solvent to kg)
57.0%=100%g)14.7+g(11.1
g14.7=100%
masstotal
solventofmass=%Mass xx
5104.30 x=10
g)14.7+g(11.1
ureag11.1=10
solutionofmass
soluteofmass=ppm 66 xx
20. Refer to Sections 10.2 and 9.3.
The compound which exhibits intermolecular forces most similar to water will be the more
soluble in water (like dissolves like). Recall that water has dispersion, dipole, and H-bonding
forces.
a. CH3Cl: dispersion forces
CH3OH: dispersion, dipole, and H-bonding forces
CH3OH would be more soluble since it shares H-bonding with water.
b. NI3: dispersion and dipole forces
KI: ionic
KI would be more soluble because it is ionic and ionic compounds generally exhibit high
solubility in water.
c. LiCl: ionic
C2H5Cl: dispersion and dipole forces
LiCl would be more soluble because it is ionic and ionic compounds generally exhibit
high solubility in water.
d. NH3: dispersion, dipole, and H-bonding forces
CH4: dispersion and dipole forcesNH3would be more soluble because of the H-bonding.
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30. Refer to Section 10.3.
The first step is to calculate the mole fraction of oxalic acid.
Hgmm0.41Hgmm21.97-Hgmm22.38- solutionOH 2 === PPP o
Hg)mm22.38)(Hgmm0.41))((4222422 OCHOHOCH
(XPXP == o
0.018422 OCH =X
Assuming 1 mole total, this means we have 0.018 mol. H2C2O4and 0.982 mol. water
(1.00 - 0.018 = 0.982). The next step is to calculate the masses associated with these
quantities, and from that the mass of solution and volume of solution.
OHg17.7=OHmol.1
OHg18.02OHmol.0.982
22
2
2
x
422
422
422422 OCHg1.6=
OCHmol.1
OCHg90.04OCHmol.0.018 x
L0.0184=mL1000
L1
g1.05
mL1solutiong1.6)+(17.7 xx
Now one can either:
1. Calculate molarity (mol./L) and convert mol./L to grams/L (using molecular mass) or
2. Directly calculate grams of H2C2O4in one liter (as shown below)
422422 OCHg87=
solutionL0.0184
OCHg1.6solutionL1.00 x
Thus, to prepare the prescribed solution, one must dissolve 87 g H2C2O4in enough water to
make 1.00 L of solution.
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40. Refer to Sections 10.3 and 3.3, and Example 10.7.
Use the freezing point depression to calculate molality, and from that, moles of the compound
and the compound's molecular mass.
Tf= Tf -Tf= 178.40C 173.44C = 4.96C
Tf= kfm
4.96C = (40.0C/m)(m)
m= 0.124 m
camphorkg.05000=g1000
kg1camphorg50.00 x
camphorkg05000.0
mol.0.124
solventkg
solutemol.
xmm ==
x= 0.00620 mol.
g/mol.403mol.0.00620
g2.50=